Origin of meiotic nondisjunction in Drosophila females.
Author(s) -
Rhoda F. Grell
Publication year - 1979
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.793133
Subject(s) - nondisjunction , genetics , meiosis , homologous chromosome , biology , chromosomal crossover , chiasma , synapsis , chromosomal translocation , loss of heterozygosity , drosophila melanogaster , bivalent (engine) , pairing , chromosome , allele , aneuploidy , gene , chemistry , physics , superconductivity , organic chemistry , quantum mechanics , metal
Meiotic nondisjunction can be induced by external agents, such as heat, radiation, and chemicals, and by internal genotypic alterations, namely, point mutations and chromosomal rearrangements. In many cases, nondisjunction arises from a reduction or elimination of crossing over, leading to the production of homologous univalents which fail to co-orient on the metaphase plate and to disjoin properly. In some organisms, e.g., Drosophila and perhaps man, distributive pairing (i.e., a psot-exchange, size-dependent pairing) ensures the regular segregation of such homologous univalents. When a nonhomologous univalent is present, which falls within a size range permitting nonhomologous recognition and pairing, distributive nondisjunction of the homologues may follow. Examples of nondisjunction induced by inversion heterozygosity, translocation heterozygosity, chromosome fragments, radiation, heat, and recombination-defective mutants are presented.
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